With the new draft regulation prepared by the Ministry of Health, it is planned to establish a comprehensive control mechanism in the food supplement sector. Regulation covering vitamins, minerals, collagen, herbal products and sports support products; It brings new rules for product content, promotional activities and sales processes. The draft study aims to clarify the classification and inspection processes of products, especially those offered for sale in drug-like forms.
Thus, it is aimed to make the distinction between food supplements and products in the pharmaceutical category more clear. A New Commission Will Be Established Within the scope of the regulation, a new structure called “Food Supplementary Evaluation and Determination Commission” will be established. The commission will examine the contents and active ingredients of the products on the market and determine which product will be subject to the inspection of which institution.
It is envisaged that products offered for sale, especially in tablet, capsule and similar forms, will be subject to a more detailed examination process. It was stated that the Turkish Medicines and Medical Devices Agency will also take an active role in the products that fall under the control of the Ministry of Health. Advertising and Promotional Activities Will Be Followed Closely The draft text includes not only product contents; It also includes increasing inspections regarding production, import, distribution and advertising processes.
It is planned to implement stricter practices, especially regarding health claims that may mislead consumers and promotions that do not have scientific basis. It was stated that due to the increase in promotions made on social media in recent years, advertising activities on digital platforms will also be included in the scope of examination. Re-Application Requirement for Existing Products According to the draft regulation, a transition period will be applied for supplementary food products currently on the market.
After the regulation comes into force, existing products will need to re-apply to the new commission within 6 months. It is envisaged that the existing permits and approvals of products that do not apply within the specified period will be deemed invalid. In this process, manufacturers and importers are expected to submit their product files for re-evaluation.
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